Domains within Homo sapiens protein KDM5A_HUMAN (P29375)

Lysine-specific demethylase 5A

Alternative representations: 1 /

Protein length1690 aa
Source databaseUniProt
Identifiers KDM5A_HUMAN, P29375, ENSP00000382688.2, ENSP00000382688, A8MV76, Q4LE72, Q86XZ1
Source gene ENSG00000073614
Alternative splicing KDM5A_HUMAN, E7EV89_HUMAN, ENSP00000443854.1, F5H322_HUMAN, F5GZR8_HUMAN

Domain architecture analysis

Display all proteins with similar:

Domain organisationProteins having all the domains as the query in the same order. Additional domains are allowed.
Domain compositionProteins with the same domain composition have at least one copy of each of the domains of the query.

Predicted functional partners

KDM5A_HUMAN is shown as KDM5A in the network

Click and drag to pan the network, and zoom by using your mouse wheel. Click the protein nodes for additional options.

The network on the left comes from STRING, a database of known and predicted protein interactions. Displayed here is the evidence view, where different line colors represent the types of evidence for the association.

Open the STRING annotation page for KDM5A

Protein KDM5A_HUMAN is possibly involved in these pathways, based on its similarity to the listed KEGG orthologous groups:

KEGG pathways

PathwayDescription
map04550Signaling pathways regulating pluripotency of stem cells

KEGG orthologous groups

KONameDescription
K11446KDM5, JARID1[histone H3]-trimethyl-L-lysine4 demethylase [EC:1.14.11.67]
K02112ATPF1B, atpDF-type H+/Na+-transporting ATPase subunit beta [EC:7.1.2.2 7.2.2.1] iPath3
Some of these orthologous groups are included in the interactive Pathways Explorer overview maps. Select an overview map and click the button below to highlight them in iPath.

Post-translational modifications

PTM annotation is taken from PTMcode, a resource of known and predicted functional associations between protein post-translational modifications (PTMs). There are 45 PTMs annotated in this protein:

PTMCount
Phosphorylation31
Ubiquitination10
Acetylation3
SUMOylation1

To see the full details, including possible functional associations between the PTMs, please visit the PTMcode annotation page for protein KDM5A.

Orthologous groups

Orthology information is taken from eggNOG, a database of orthologous groups of genes. Orthologous groups containing this protein are listed below. This protein is named 9606.ENSP00000382688 in eggNOG.

OGTaxonomic classDescription
LCOG0055All organisms (root)F-type H+/Na+-transporting ATPase subunit beta [EC:7.1.2.2 7.2.2.1],[histone H3]-trimethyl-L-lysine4 demethylase [EC:1.14.11.67],F-type H+-transporting ATPase subunit beta [EC:7.1.2.2]
KOG1246Eukaryota (superkingdom)[histone H3]-trimethyl-L-lysine4 demethylase [EC:1.14.11.67],protein Jumonji,lysine-specific demethylase 6A [EC:1.14.11.68]
HT2GHMetazoa (kingdom)[histone H3]-trimethyl-L-lysine4 demethylase [EC:1.14.11.67],guanine nucleotide exchange factor
94B3DChordata (phylum)[histone H3]-trimethyl-L-lysine4 demethylase [EC:1.14.11.67],guanine nucleotide exchange factor
5RCZZSarcopterygii (superclass)[histone H3]-trimethyl-L-lysine4 demethylase [EC:1.14.11.67]
8Z880Mammalia (class)[histone H3]-trimethyl-L-lysine4 demethylase [EC:1.14.11.67]
4RAEFEuarchontoglires (superorder)[histone H3]-trimethyl-L-lysine4 demethylase [EC:1.14.11.67]
4ZNJDPrimates (order)[histone H3]-trimethyl-L-lysine4 demethylase [EC:1.14.11.67]
98N8EHaplorrhini (suborder)[histone H3]-trimethyl-L-lysine4 demethylase [EC:1.14.11.67]
BV4RYSimiiformes (infraorder)[histone H3]-trimethyl-L-lysine4 demethylase [EC:1.14.11.67]
9ERVBCatarrhini (parvorder)[histone H3]-trimethyl-L-lysine4 demethylase [EC:1.14.11.67]
H6EHGBilateria (clade)[histone H3]-trimethyl-L-lysine4 demethylase [EC:1.14.11.67],guanine nucleotide exchange factor
7P283Opisthokonta (clade)[histone H3]-trimethyl-L-lysine4 demethylase [EC:1.14.11.67],guanine nucleotide exchange factor
9GB3GVertebrata (clade)[histone H3]-trimethyl-L-lysine4 demethylase [EC:1.14.11.67],guanine nucleotide exchange factor

The SMART diagram above represents a summary of the results shown below. Domains with scores less significant than established cutoffs are not shown in the diagram. Features are also not shown when two or more occupy the same piece of sequence; the priority for display is given by SMART > PFAM > PROSPERO repeats > Signal peptide > Transmembrane > Coiled coil > Low complexity. In either case, features not shown in the above diagram are listed in the right side table below, and the reason for their omission is shown in the 'Reason' column.

Confidently predicted domains, repeats, motifs and features:

Outlier homologues and homologues of known structure:

Features NOT shown in the diagram: